BfArM - Federal Institute for Drugs and Medical Devices

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Information Letter on Eligard® (leuprorelin acetate depot injection): Risk of lack of efficacy due to incorrect reconstitution and administration PDF, 521KB, File is accessible Date: 28. November 2014 Topics: Pharmakovigilanz Type: Direct Healthcare Professional Communication

Active substance: leuprorelin acetate

The company Astellas Pharma GmbH is circulating information on a possible lack of clinical efficacy that may occur if the product is reconstituted incorrectly.

Counterfeit medicinal products in Spain Date: 26. November 2014 Topics: Pharmakovigilanz Type: Risk information

Active substance:

On 18 November 2014, the Spanish licensing authority Agencia Española de Medicamentos y Productos Sanitarios (AEMPS--Agencia Española de Medicamentos y Productos Sanitarios) issued information on initial findings on illegally traded medicinal …

Dear Doctor Letter (Rote-Hand-Brief) on Fenistil® 1 mg/ml solution for injection (dimethindene maleate): Quality defects; recall of two batches PDF, 483KB, File is accessible Date: 25. November 2014 Topics: Pharmakovigilanz Type: Direct Healthcare Professional Communication

Active substance: dimethindene maleate

The company Novartis Consumer Health GmbH is sending out information on the recall of batches 11027154 and 11045012 of the medicinal product Fenistil® 1 mg/ml solution for injection as the vials of both batches partially exhibit leakage at the …

Medicinal products that affect the renin-angiotensin(-aldosterone) system (RAS/RAAS): realisation of the EU Commission's implementing decision Date: 13. November 2014 Topics: Pharmakovigilanz Type: Risk Assessment Procedures

Active substance: ACE-Hemmer | Angiotensin-II-Rezeptor-Antagonisten | Aliskiren

In its notice of 31 October 2014, the Federal Institute for Drugs and Medical Devices (BfArM) has ruled the realisation of the corresponding implementing decision (2014) 6371 of the EU Commission.

Information letter on medicinal products containing codeine as liquid dosage forms by UCB Pharma GmbH: Recall Date: 13. November 2014 Topics: Pharmakovigilanz Type: Direct Healthcare Professional Communication

Active substance: codein

The company UCB Pharma GmbH is circulating information on the recall of medicinal products containing codeine as liquid dosage forms.

Levonorgestrel- and ulipristal acetate-containing medicines for emergency contraception: influence of body weight/BMI on efficacy/bioavailability Date: 07. November 2014 Topics: Pharmakovigilanz Type: Risk Assessment Procedures

Active substance: levonorgestrel | ulipristal acetate

In its notice of 5 November 2014, the Federal Institute for Drugs and Medical Devices (BfArM) has ruled the realisation of the corresponding implementing decision C(2014)7147of the EU Commission.

Tecfidera® (dimethyl fumarate): First case of progressive multifocal leukoencephalopathy (PML) Date: 07. November 2014 Topics: Pharmakovigilanz Type: Risk information

Active substance: dimethyl fumarate

At the request of the BfArM, the Pharmacovigilance Risk Assessment Committee (PRAC) discussed a fatal case of progressive multifocal leukoencephalopathy (PML) which was reported in a patient treated with Tecfidera® (dimethyl fumarate) at its …

Information letter on Xofigo® (radium 223 dichloride): Temporary shortage of the medicinal product and special temporary preparation instructions. PDF, 75KB, File is accessible Date: 07. November 2014 Topics: Pharmakovigilanz Type: Direct Healthcare Professional Communication

Active substance: radium-223-dichlorid

The company Bayer Vital GmbH is circulating information on a worldwide temporary shortage of the medicinal product Xofigo® as recently produced batches did not pass routine quality checks prior to release.

Information Letter on Xofigo® (radium 223 dichloride): Temporary shortage of the medicinal product PDF, 2MB, File is accessible Date: 05. November 2014 Topics: Pharmakovigilanz Type: Direct Healthcare Professional Communication

Active substance: radium-223-dichlorid

The company Bayer Vital GmbH is circulating information on a worldwide temporary shortage of the medicinal product Xofigo® as recently produced batches did not pass routine quality checks prior to release.

Dear Doctor Letter (Rote-Hand-Brief) on Beofenac® (aceclofenac): New contraindications and warnings PDF, 1MB, File is accessible Date: 28. October 2014 Topics: Pharmakovigilanz Type: Direct Healthcare Professional Communication

Active substance: aceclofenac

The company Almirall Hermal GmbH is circulating information that treatment with aceclofenac - similar to that with diclofenac and selective COX-2 inhibitors - is associated with an increased risk of arterial thrombotic events.